Sustained release drug delivery system

ABSTRACT

Disclosed is a controlled release dosage form comprising a therapeutically effective amount of a pharmaceutically active agent, which may be Acyclovir, that releases in about 12 hours 80-100% of the active agent in a simulated gastric juice in a first order rate of release in a USP type 2 dissolution test, and not containing a solubilizer or a swelling enhancer or both, containing (a) a tablet made from polymer matrix of at least two biocompatible polymers, which may be Carbopol 974P and polyethylene oxide, the pharmaceutically active agent and pharmaceutically permitted excipients; the tablet capable of rapid swelling without disintegration in the simulated gastric juice to a size that results in its gastric retention in the stomach and start controlled release of the active agent by starting controlled erosion as well as diffusion immediately after coming into contact with the gastric juice.

INCORPORATION BY REFERENCE TO ANY PRIORITY APPLICATIONS

Any and all applications for which a foreign or domestic priority claim is identified in the Application Data Sheet as filed with the present application are hereby incorporated by reference under 37 CFR 1.57.

BACKGROUND OF THE INVENTION

Field of the Invention

The present invention describes sustained/controlled drug delivery system so as to increase the bioavailability of a drug use of mucoadhesive, swelling polymers and their derivatives as a carrier for achieving sustained/controlled drug delivery, particularly for the drug acyclovir and the mucoadhesive swelling polymers like Carbopol, PEO, Sodium alginate, Hypromellose, hydroxypropyl cellulose, sodium carboxy methyl cellulose, Eudragits, Chitosan and its derivatives.

Description of the Related Art

Some of the drug and macromolecules are poorly absorbed across the mucosal membrane or those that are sparingly/slowly soluble resulting in the fact that during limited time they remain in the gastrointestinal tract, enough of them is not released or absorbed and major portion passes out unabsorbed. One of the greatest challenge to the scientists is drug delivery of such molecules which show poor bioavailability as limited amount of the dose reaches the plasma in a specified period. Low bioavailability leads to variation in the drug absorption amongst the patients and become very difficult to administer the effective dosage. Hence, it has been a long awaited requirement of the drug delivery scientists to enhance the bioavailability of the such orally administered drugs. It was thought that a carrier which can deliver drug in intact form at target site, stays there for prolonged time and increases the permeability of the mucosal membrane to achieve unhampered and better absorption of the drug shall be a remedy, provided the carrier is safe and does not affect the properties of the mucosal epithelium. Acyclovir, one of the subject matters of present invention is a drug in this category: poorly water soluble, has poor and variable oral bioavailability (10-20%), the elimination half-life of aciclovir is approximately 3 hours, is renally excreted, partly by glomerular filtration and partly by tubular secretion.

The present invention deals with carriers, including but not limited to polymers like chitosan (and its derivatives not limited to Thiolated chitosan, Trimethyl chitosan, hypermellose, polyethylene oxide, Carbopol, sodium alginate, sodium carboxymethyl cellulose, xanthan gum and similar products, derivatives of these polymers, their various combinations and the like which are mucoadhesive, swellable and which increases the G.I. retention, bioavailability of the drug during the delivery.

Prior Art

Genta et al.¹ (1997)₁ have described use of microparticles of polylactides and polylactide-co-glycolide to achieve sustained delivery of acyclovir.

Thanau et al.² (2001) have extensively reviewed methods of use of chitosan and trimethyl chitosan as absorption enhancers of hydrophilic macromolecular drugs including peptide drugs. The experiments conducted in pigs and rats showed increased bioavailability of a peptide drug.

There are several examples of use of thiolated chitosan and TMC as drug delivery vehicle of macromolecular polymeric drugs such as insulin, laminin peptide, FITC-dextran 4000 as model lipophilic drug³⁻⁵.

Grafted chitosans have been used as absorption enhancers in drug delivery systems.

Rokhade et al.⁶ (2007) have described semi-interpenetrating polymer network (IPN) of microspheres of acrylamide grafted on dextran and chitosan prepared by emulsion cross-linking method using glutaraldehyde as a cross linker and encapsulation of acyclovir into the microspheres and drug release was found to be extended up to 12 hours. They have, however, used the drug theophylline and its physicochemical properties are totally different than Acyclovir in view of the fact that its bioavailability is 100%.

Hu et al.⁷ (2009) have used stearic acid grafted chitosan oligosaccharide which form micelle wherein the drug is incorporated for improved absorption of the drug Doxorubicin.

U.S. Pat. No. 6,340,475⁸ discloses a controlled-release oral drug dosage form for releasing a drug whose solubility in water is greater than one part by weight of said drug in ten parts by weight of water, said dosage form comprising a solid polymeric matrix with said drug dispersed therein at a weight ratio of drug to polymer of from about 15:85 to about 80:20, said polymeric matrix being one that swells upon imbibition of water thereby attaining a size large enough to promote retention in the stomach during said fed mode, that releases said drug into gastric fluid by the dissolution and diffusion of said drug out of said matrix by said gastric fluid, that upon immersion in gastric fluid retains at least about 40% of said drug one hour after such immersion and releases substantially all of said drug within about eight hours after such immersion, and that remains substantially intact until all of said drug is released. In other claims that pertain to several groups and examples of drugs, the claims limit the period required for release of substantially all of the said drug to within about 10 hours. In this patent the dosage form is designed for treating the local disease of stomach like Ulcer not for systemic absorption.

US 20040185105⁹ discloses a controlled release dosage form comprising a polymer matrix and a pharmacologically active agent dispersed in the said polymer matrix comprised of a biocompatible, hydrophilic polymer where the dosage form upon imbibition of water swells unrestrained dimensionally to a size effective to promote gastric retention and maintains its size for an extended period of time before it is diminished by erosion.

US20070160678¹⁰ discloses the invention of microcapsules of polymer insoluble in GIT fluid. The in vivo release pattern of acyclovir has also been described. Invention showed that 80% acyclovir was released in first 3 hrs. There is no information on the bioavailability and reduction of dosing frequency.

None of the above cited references describe in vivo studies conducted to know exactly how the drug works in the in vivo atmosphere. The present invention along with disclosure on novel and improved ways to use of various mucoadhesive carriers used to deliver drugs having low bioavailability describes in vitro as well as in vivo studies on controlled release compositions conducted and illustrated more particularly on a drug acyclovir entrapped in chitosan, thiolated chitosan and Trimethyl chitosan or acyclovir associated with other polymers to achieve an objective of improving the uniformity of drug release and to increase the period for which the drug is released from the dosage form. The methods and compositions of this invention illustrated on Acyclovir are applicable on any other drug having same or similar properties as well as problems in the context of drug delivery, efficacy and treatment.

SUMMARY OF THE INVENTION

The invention discloses a controlled release dosage form comprising a therapeutically effective amount of a pharmaceutically active agent that would release in about 12 hours 80-100% of the said active agent in a simulated gastric juice in a first order rate of release in a USP type 2 dissolution test, and not containing a solubilizer or a swelling enhancer or both, comprising (a) a tablet made from polymer matrix of at least two biocompatible polymers, at least one of which is mucoadhesive, the said pharmaceutically active agent and pharmaceutically permitted excipients; the said tablet capable of rapid swelling without disintegration in the said simulated gastric juice to a size that shall result in its gastric retention in the stomach and start controlled release of the said active agent by starting controlled erosion immediately after coming into contact with the said gastric juice, or (b) microspheres of ungrafted chitosan or a chitosan derivative, or Carbopol incorporating the said active agent, wherein the said pharmaceutically active agent is not a polymeric molecule and after administration in stomach, the said microspheres adhere to the gastric mucosa for a long time releasing the active agent in a controlled way. The two polymers illustrated in the tablet of this invention are Carbopol 974P and Polyethylene oxide; however, any other pair of polymers can be used that shall result, in an appropriate proportion that have the drug release characteristics defined above. The permitted pharmaceutical excipients of this invention comprise a binder, a diluent, a pH modifier, a glidant, a lubricant, a film former, an anti-adherent, a coating agent, a colorant.

In one particular illustration of this invention, the tablet comprises Acyclovir, Carbopol 974P, Polyethylene oxide, Avicel PH 101, Povidone K30, Magnesium stearate, and Colloidal silicon oxide. More particularly, the said tablet contains following ingredients for every 1000 mg of the dosage form: Acyclovir 763.37 mg, Carbopol 974P 75 mg, Polyethylene oxide 25 mg, Avicel PH 101 93.83 mg, Povidone K30 30 mg, Magnesium stearate 7.5 mg, Colloidal silicon oxide 5.0 mg.

The chitosan derivative used in making microspheres comprise Trimethyl chitosan or Thiolated chitosan. Mixtures may also be used, if expedient to achieve the desired drug release profile.

The microspheres of this invention may be packed in a sachet or are used as an ingredient with optional addition of permitted pharmaceutical ingredients and excipients to make a solid unit dosage form comprising a tablet or/and a capsule.

This invention also discloses a method of orally administering a therapeutically effective amount of a pharmaceutically active agent from a controlled release dosage form to a patient, the said dosage form would release in about 12 hours 80-100% of the said active agent in a simulated gastric juice in a first order rate of release in a USP type 2 dissolution test, and not containing a solubilizer or a swelling enhancer or both, comprising (a) a tablet made from polymer matrix of at least two biocompatible polymers, the said pharmaceutically active agent and pharmaceutically permitted excipients; the said tablet capable of rapid swelling without disintegration in the said simulated gastric juice to a size that shall result in its gastric retention in the stomach and start controlled release of the said active agent by starting controlled erosion immediately after coming into contact with the said gastric juice, or (b) microspheres of ungrafted chitosan or a chitosan derivative incorporating as the said active agent, wherein the said pharmaceutically active agent is not a polymeric molecule and after administration in stomach, the said microspheres adhere to the gastric mucosa for a long time releasing the active agent in a controlled way.

The polymers used in the method of this invention illustrated in this invention comprise Carbopol 974P and Polyethylene oxide. However, any other pair of polymers providing the defined drug release profile as above may be used in their place. The pharmaceutical active illustrated for method of this invention is Acyclovir. However, any other pharmaceutically active agent with same properties as Acyclovir and same drug release problems as Acyclovir may be used in its place.

The permitted pharmaceutical excipients used in the method of this invention comprise a binder, a diluent, a pH modifier, a glidant, a lubricant, a film former, an anti-adherent, a coating agent, a colorant.

The controlled release dosage form of the method of this invention comprises Acyclovir, Carbopol 974P, Polyethylene oxide, Avicel PH 101, Povidone K30, Magnesium stearate, Colloidal silicon oxide, Ethanol.

In a particular embodiment of method of this invention, every 1000 mg of the dosage form the said controlled release dosage form comprises Acyclovir 763.37 mg, Carbopol 974P 75 mg, Polyethylene oxide 25 mg, Avicel PH 101 93.83 mg, Povidone K30 30 mg, Magnesium stearate 7.5 mg, Colloidal silicon oxide 5.0 mg. Chitosan derivative used in making microspheres of this invention comprises Trimethyl chitosan or/and Thiolated chitosan.

This invention also comprises a method wherein the said microspheres are packed in a sachet or are used as an ingredient with optional addition of other pharmaceutically permitted ingredients and excipients to make a solid unit dosage form comprising a tablet and a capsule.

A process of making oral dosage form of this invention comprises, for tablet form, the steps of making wet granulation of a mixture comprising the said pharmaceutically active ingredient, the polymers and excipients, adding a glidant and pressing into a tablet.

A process for making microspheres of this invention comprises preparing a solution of chitosan or a chitosan derivative in acetic acid, adding aqueous solution of the pharmaceutically active agent, adding this mixture to continuous phase consisting of light liquid paraffin and heavy liquid paraffin (1:1) containing a surfactant under constant stirring to form a water-in-oil emulsion, adding gluteraldehyde drop wise over a period of time, continuing stirring for a period of time, separating the microspheres formed by centrifugation, washing with petroleum ether to remove liquid paraffin, suspending in a sodium bisulfite solution and stirring for a period of time to remove residual gluteraldehyde, washing finally with distilled water, drying the microspheres.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1. SEM photomicrograph of Chitosan (A), N-TMC (B), Thiolated chitosan (C), Carbopol (D) and Methocel K15M (E) microsphere (×10,000). Scale bar=50 μm

FIG. 2. % Swelling measurement of microspheres formulations. Data are represents as mean±SD (n=3)

FIG. 3. % In vitro drug release of acyclovir from microspheres formulations. Data are represented as mean±SD (n=3)

FIG. 4. Penetration of 6-CF (1 ml of 0.3% w/v) as fluorescence probe across the duodenum section of intestinal mucosa after 3 hr administration as solution (A), thiolated chitosan (B), TMC (C), chitosan (D), Carbopol (E) and Methocel K15M (F) microsphere formulation (×450). Scale bar=250 μm; MU=Mucosal surface; VI=Villi.

FIG. 5. Plasma concentration of acyclovir after administration as drug solution and microsphere formulations. Data are represents as mean±SD (n=3)

FIG. 6. Showing plasma concentration-time profile of this simulation

FIG. 7. Showing the comparison of simulated plasma concentration-time profiles of Acyclovir IR 200 mg & 400 mg

FIG. 8. Plasma levels of multiple dose administration of Acyclovir IR 200

FIG. 9. Shows the comparison of plasma concentrations of Acyclovir IR 200 mg during the dosing day on day 1 and day 5.

FIG. 10. Comparative plasma concentration profiles of acyclovir immediate release and acyclovir controlled release tablets.

FIG. 11. Predicated in vitro drug release profile of Acyclovir CR formulation

FIG. 12. In vitro drug release profile from gastroretentive tablets prepared using Carbopol 974P as polymer (Batch Acy-ER-1A & Acy-ER-1B).

FIG. 13. In vitro drug release profile from gastroretentive tablets prepared using Polyethylene oxide (Batch Acy-ER-2A & 2B).

FIG. 14. In vitro drug release profile from gastroretentive tablets prepared using combination of Carbopol 974P and Polyethylene oxide (Batch 3A, 3B & 3C).

FIG. 15. Comparative In vitro drug release profile from different batches of gastroretentive tablets and target release profile for sustained release acyclovir formulation generated by computer simulation study.

FIG. 16. % Swelling profile from different batches of gastroretentive tablets.

FIG. 17. Mucoadhesive strength measurement of different batches of gastroretentive tablets.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT

The polymer/s of present invention include water soluble or water insoluble one/s, further including chitosan and chitosan derivatives exemplified by thiolated chitosan and trimethyl chitosan, Carbopol, HPMC, alginates, pectins, Eudragits, Hypromellose, polyethylene oxide their combinations and the like. The pharmaceutically acceptable excipient of present invention may be selected from the group of binder, diluent, pH modifier, glidant, lubricant, film formers, anti-adherent, coating agents colorant and the like.

The sustained release delivery system may be in the form of single or multiple units. It can be in the form of tablets, capsules, microspheres, pellets, granules, and like. It can be packed in blister, bottles, sachets and like.

The delivery system may be prepared by the processes well known in the art of formulation development, such as wet granulation, dry granulation, direct compression, blending, extrusion & spheronization, coating and the like.

The sustained release delivery system of present invention may be administered as the dosage required by the patient.

The present invention also deals with pharmacokinetic simulations for a drug, more particularly Acyclovir controlled release (CR) to:

-   -   determine the dose and absorption rate required for Acyclovir CR         to achieve comparable C_(max) and C_(min) with that of immediate         release (IR).     -   predict the blood levels of Acyclovir CR and compare with that         of IR.     -   simulate in-vitro dissolution profiles from absorption rate         constants.

One of the polymer used for sustained release is Chitosan which is a polysaccharide comprising copolymers of glucosamine and N-acetyl glucosamine. It is biodegradable, biocompatible, mucoadhesive polymer and has been used in the formulation of particulate drug delivery system. Chitosan opens the epithelial tight junctions in concentration and pH dependent way. At acidic pH, chitosan is effective in increasing the permeability of certain drugs, but as the pH increases, its effectiveness is decreased.¹¹

So, to overcome the solubility limitations of chitosan at increased pH values, an N-Trimethyl quartenized chitosan (N-TMC) derivative was synthesized and used for comparison studies. N-TMC has shown potential as an absorption enhancer across intestinal epithelial cells even in neutral environments.² The mechanism of drug absorption enhancement by N-TMC is the same as that of chitosan.¹² It opens the tight junctions between the adjacent epithelial cells by means of interaction between the positive charges on the polymer molecules and the anionic components on the surface of epithelial cells.

Another polymer selected in the present study is thiolated chitosan. Thiolated chitosan represents a new promise in the field of mucoadhesive polymers. The higher mucoadhesive properties of thiomers are reported to intensify the contact with gastric mucosa, providing an increased epithelial permeability for many drugs.¹³⁻¹⁵ In addition, these polymers are reported to increase the intestinal permeability of drugs that shall be beneficial for increasing the intestinal permeability of acyclovir along with mucoadhesiveness.

In one of the embodiment of this invention drug Acyclovir which is used for the treatment of herpes simplex virus infections, is most widely used drug for infections such as cutaneous herpes, genital herpes, chicken pox, varicella zoster infections and herpes keratitis.¹⁶ Acyclovir is currently marketed as capsules, tablets and suspension for oral administration, intravenous injection and topical ointment. Oral acyclovir is mostly used in dose strength as 200 mg tablets, 5 times a day. In addition, long term administration of acyclovir (six month or longer) is required in immunocompetant patient with relapsing herpes simplex infection.¹⁷ The presently available conventional therapy is associated with a number of drawbacks such as highly variable absorption and low bioavailability (10-20%) and requirement of frequent administration (5 times a day) resulting in poor patient compliance. Furthermore, with increase in dose, there was seen decrease in bioavailability. Moreover, the mean plasma half life of the drug being 2.5 hrs, necessitates repeated administration of high dose of the drug (200 mg five times a day). As a result, most of the drug is excreted in the faeces (50-60%) in unabsorbed form.¹⁸ Acyclovir is soluble in acidic pH and is predominantly absorbed from upper regions of gastro intestinal tract (GIT).¹⁹

One of the embodiment of the present investigation discloses mucoadhesive microspheres for gastroretentive delivery of a drug. Polysaccharide Chitosan, thiolated chitosan, Trimethyl Chitosan, Carbopol 71G and Methocel K 15M and their various combinations were used as mucoadhesive polymers. Microsphere formulations were prepared using emulsion-chemical crosslinking technique and evaluated in vitro, ex-vivo and in-vivo. These microspheres may be administered in dosage forms, including a sachet, as a tablet, through a capsule and the like.

Another embodiment, discloses gastroretentive tablets of acyclovir were prepared from one or more the polymers and excipients for sustained delivery.

In further embodiment of this invention the drug pharmacokinetic simulation was done for Acyclovir CR to:

-   -   determine the dose and absorption rate required for Acyclovir CR         to achieve comparable C_(max) and C_(min) with that of IR.     -   predict the blood levels of Acyclovir CR and compare with that         of IR.     -   simulate in-vitro dissolution profiles from absorption rate         constants.

In the following are described experiments conducted that serve as non limiting illustrations of how the invention is performed. Any modifications or variations in the parameters including but not limited to polymers used, their combination used, drugs used, chemicals and their concentrations used, various procedures for assaying the drug, simulation of the drug are merely illustrative and any equivalents of them that are obvious to a person skilled in the art and that are capable of achieving the same objective if used in their place shall be considered as included in the content/scope of this specification

Materials and Methods Materials

Chitosan (degree of deacetylation 82% and molecular weight 650,000) was obtained as gift sample from Central Fisheries Research Institute, Cochin. Methocel K15M and Carbopol 71G were obtained as gift sample from Colorcon Ltd., Mumbai and Degussa Ltd., Mumbai, respectively. 2-Iminothiolane-HCl, 6-Carboxyfluorescein (6-CF) and Traut's reagent were procured from Sigma-Aldrich Ltd., USA. Ethanol, acetonitrile, methanol and xylene were procured from E. Merck Ltd., Mumbai, India. Thiolated Chitosan and N Trimethyl chitosan (N-TMC) was prepared in the lab according to the method reported by Bernkop-Schnurch et al.¹⁴.

Preparation of Microspheres Formulations

Microspheres formulations using chitosan, N-TMC and thiolated chitosan as polymers were prepared using the emulsification cross linking method (Wang et al.²⁰). Emulsification cross linking method was optimized for different process and formulation variables.

A solution of chitosan, (1.0 to 2.0% w/v) was prepared in acetic acid (2% v/v) and aqueous solution of drug (0.1 to 0.5% w/w) was added to their respective solution. This was further added to continuous phase (consisting of light liquid paraffin and heavy liquid paraffin (1:1) containing Span 80 (0.5% w/v) as surfactant) under constant stirring (1200-2000 rpm) using a three blade propeller stirrer to form w/o emulsion. This was followed by addition of gluteraldehyde (0.25 to 1.0 ml, 25% v/v) drop wise at 15, 30, 45 and 60 min, respectively. The stirring was continued for 3.5 hours. The microspheres so obtained were separated by centrifugation and washed with petroleum ether to remove liquid paraffin. The microspheres were suspended in 5% w/v sodium bisulfite solution and stirred for 15 minutes to remove residual gluteraldehyde. Final washing was done with distilled water, microspheres were dried and stored in a vacuum desiccator. Thiolated chitosan and N-Trimethyl chitosan microsphere was prepared using same method using optimized process and formulations variables.

Microspheres of Carbopol 71G and Methocel K15M were prepared by spray drying techniques as reported by Harikarnpakdee et al.²¹ Methocel K15M or Carbopol 71G were dissolved in deionised water. Acyclovir was separately dissolved in distilled water. Colloidal silicon dioxide (Aerosil), maltodextrin and propylene glycol were then mixed with the polymer solution. The solution of each batch was spray dried employing inlet temperature of 120° C. for Carbopol 71G and 130° C. for Methocel K15M, pump setting of 5 ml/min; spray flow rate of 400 nano liter/min.

Fluorescently loaded microspheres were prepared in the same way. For this purpose drug solution was replaced with 0.3% w/v solution of 6-CF and microspheres were prepared using the procedure described above.

Characterization of Microspheres Morphological Examination

The morphology of microspheres was examined by scanning electron microscopy (SEM, JSM-5310LV scanning microscope Tokyo, Japan). The microspheres were mounted on metal stubs using double-sided tape and coated with a 150° A layer of gold under vacuum using gold coater. Stubs were visualized under scanning electron microscope.

Particle Size Measurement

The particle size of the microspheres was measured using stage micrometer scale. Dry microspheres (5 mg) were suspended in distilled water and ultrasonicated for 5 seconds. A drop of suspension was placed on a clean glass slide and microspheres were counted under stage ocular micrometer. Minimum of 200 microspheres were counted per batch.

Swelling Measurement

The swelling of microspheres was conducted in phosphate buffer pH 6.8. The size of dried microsphere and after incubating in phosphate buffer (pH 6.8) for 0.3, 1.0, 3.0 and 5.0 hr was measured by using microscopic method. The percentage of swelling at different time interval was determined by taking difference between diameter of microspheres at time t (D_(t)) and initial time (t=0 [D₀]) as calculated from the following equation

Swelling %=D _(t) −D ₀ /D ₀*100   (1)

Production Yield

The production yield (% w/w) was calculated from the ratio of average weight of dried microspheres (W1) recovered from each of three batches to the sum of initial dry weight of starting materials (W2).

Entrapment Efficiency

Acyclovir loaded microspheres (10 mg) of chitosan, N-TMC or thiolated chitosan were digested in HCl (0.01M). Carbopol 71G and Methocel K15M microspheres were dispersed in 0.1M NaOH and 0.05M phosphate buffer (pH 6.8), respectively for overnight with intermittent shaking. The mixture was filtered and filtrate was assayed spectrofluorometrically (Elico Spectrofluorometer, SL-174, Delhi, India) at excitation wavelength of 256 nm and emission wavelength of 374 nm according to the method reported by Darwish et al.²² The entrapment efficiency was calculated from the ratio of actual amount of the drug present in the formulation to the initial amount of the drug added

Mucoadhesion Measurement Study

The mucoadhesion property of microsphere formulations was determined according to the method described by Vyas et al.²³ A 5 cm long piece of freshly cut pig intestine was obtained from a local abattoir within 1 hr of killing of animal was further cleaned by washing with isotonic saline solution. An accurate weight of microspheres was placed on the mucosal surface to which was attached a polyethylene plate that was fixed at an angle of 40° relative to the horizontal plane. Phosphate buffer (pH 6.8) warmed at 37±1° C. was flown at a rate of 5 ml/min over the tissue. The time required for detaching all the microspheres from mucosal surface of the pig intestine was recorded by visual inspection.²¹

In Vitro Drug Release Study

In vitro release of acyclovir from microspheres was determined by carrying out dissolution test using USP paddle method at a stirring rate of 50±5 rpm at temperature 37±0.5° C. 900 ml of HCl buffer (pH 1.2) was used as dissolution medium for first hr and phosphate buffered saline (PBS, pH 6.8) was used for next 11 hrs. The dried microspheres were filled in hard gelatin capsules and were placed in dissolution vessels. 5 ml sample was withdrawn at various time intervals and volume of the media was replenished with an equal amount of dissolution media. The samples were then analyzed spectroflurometrically.

G.I.T Distribution

Rats (Sprague dawley strain), 6 to 8 months old, weighing 200-220 gm were kept on fasting for 16-20 hr before commencement of the experiment. Water was provided ad libitum. The protocols for these investigations were approved by the Institutional Animal ethics committee in accordance with the disciplinary principles and guidelines of CPCSEA. Six groups were employed in the present study with each group containing 15 rats. First group received oral administration of aqueous solution of 6-CF (1 ml of 0.3% w/v). The second, third, fourth, fifth and sixth groups received microsphere of 6-CF prepared from chitosan (M-CH), thiolated chitosan (M-TCH), N-Trimethyl chitosan (N-TMC), Carbopol 71G or Methocel K15M, respectively. Oral administration of microspheres was accomplished by suspending 20 mg sample of microspheres corresponding to 3.0 mg of 6-CF in 1.0 ml normal saline and force-feeding via a rubber tube under non-anesthetic conditions. The rats were sacrificed after 2, 4, 6, 8 or 10 hr of administration, stomach (section 1) along with entire length of small intestine that was further subdivided into 6 sections (sections 2-7; length of each section 14 cm) were isolated immediately. The stomach and intestinal sections were cut opened to expose the inner mucosal surface. All microspheres located in each part were collected by scratching the mucosa with a spatula. To the collected sample, 10 ml of 0.1 N HCl was added in case of chitosan, thiolated chitosan and N-TMC. The 0.1 N NaOH and phosphate buffer (0.05 M) were added in case of Carbopol 71G and Methocel K15M microsphere, respectively. The mixture was mashed using homogenizer to extract 6-CF and kept for 24 hr. After centrifugation at 3000 rpm for 20 min, the supernatant was analyzed fluorometrically at λ_(exitation) 489 nm and λ_(emmission) 515 nm for 6-Carboxyfluorescein. The extraction efficiency of 6-CF using this method was found to be approximately 95%. In addition a 2 cm portion of section 2, 3 and 4 was taken out and further processed for fluorescence microscopy.

Fluorescence Microscopy

Fluorescence microscopy was performed to determine the extent of distribution and penetration of microsphere formulations. The excised tissue sections of GIT were blotted with tissue paper. The wiped tissue was fixed in fixative solution (3:1 absolute alcohol:chloroform) for 3 hr. The pieces were first transferred to absolute alcohol for 0.5 hr and then in absolute alcohol and xylene for 1 hr. Wax scrapings were added in this solution till saturation and were kept for 24 hr. Paraffin blocks were made by embedding the tissue in hard paraffin, matured at 62±1.0° C. The sections (5 μm thickness) were cut using microtome (Erma optical works, Japan) and examined under fluorescence microscope (Leica, DMRBE, Bensheim, Germany).

Hemolytic Toxicity Assay

The procedure from literature was followed to perform the hemolytic toxicity studies.¹⁹ Blood from healthy donors was collected and anticogulated with 3% sodium citrate. Erythrocytes were separated from blood plasma by centrifugation (3000×g, 5 min) and suspended in phosphate buffer saline (PBS) of pH 7.4. The RBC suspension (1%) was mixed with distilled water, which was considered as producing 100% hemolysis, and normal saline producing no hemolysis hence acting as blank. 0.5 ml 2% w/v dispersion of microspheres formulations in PBS (pH 7.4) was added to 4.5 ml of normal saline and interacted with 1 ml RBC suspension. Similarly, 0.5 ml of 0.3% w/v solution of acyclovir in PBS were mixed with 4.5 ml of normal saline and interacted with RBC suspension and kept in incubator for 1 hr at 37±1.0° C. After 1 hr, mixture was centrifuged and supernatants were taken and diluted with an equal volume of normal saline and absorbance was taken at 540 nm against supernatant of normal saline diluted similarly as blank. The percentage hemolysis was thus determined for each sample by taking absorbance of water as 100% hemolytic sample.

Pharmacokinetic Study

Rats (Sprague dawley), 6 to 8 months old, weighing 200-220 gm were divided into 6 groups, each consisting of 5 animals. Rats were kept on fasting 12 hours before drug administration and until 24 hours post dosing. Water ad libitum was given throughout the study. The dose selected of acyclovir was 5 mg/kg.²⁴ First group received oral administration of 0.3% w/v drug solution in PBS (pH 7.4). Second, third, fourth, fifth and sixth group received oral administration of chitosan, thiolated chitosan, trimethyl chitosan, Carbopol or Methocel microspheres, respectively. A 20 mg sample of microsphere corresponding to 3.0 mg of acyclovir were suspended in 1.0 ml saline and administered orally using a rubber tube under non-anesthetic condition. At 2.5, 5, 10, 15 and 24 hrs time intervals, blood was collected from jugular vein in ependorff tubes and centrifuged at 2000 rpm for 10 min (REMI Equipment, Mumbai, India). Supernatant was collected and acetonitrile was added to precipitate the proteins. The precipitated proteins were settled by centrifugation at 2000 rpm for 15 min. The supernatant was collected and filtered through a 0.45 μm filter into volumetric flask and drug concentration was determined by spectrofluoremetric assay.

Pharmacokinetic Simulations Performed for Acyclovir Controlled Release

Assumptions considered for simulation performance study are as follows:

-   -   1. The product will be indicated for initial and intermittent         therapy of genital herpes. These conditions require a dosage of         200 mg every four hours, 5 times daily for 10 days.     -   2. The product will be a bioadhesive dosage form, which would be         designed to be retained in upper part of GIT for a prolonged         period of time.     -   3. The CR formulation will be administered two times a day.     -   4. Bioavailability of CR formulation is 25% higher than that of         IR formulation due to prolonged residence in absorbable areas of         GIT.     -   5. The absorption process is controlled by the release from the         dosage form. The intrinsic absorption rate constant of the drug         is far higher than the drug release from the dosage form         (Ka>>>>>>>drug release rate) and hence absorption of any amount         of drug release from the dosage form is instantaneous.

Simulations Performed

The simulation process involved following steps.

-   -   1. As a first step the plasma concentration profiles of         Acyclovir/Acyclovir IR tablets were calculated using the         pharmacokinetic parameters reported in the literature¹⁶⁻¹⁸.     -   2. These parameters were then used to calculate required         properties of CR dosage form.     -   3. Then simulations for CR dosage form were performed using         parameters obtained in step 2.         The methodology and results are summarized in table 6-9 and FIG.         6-11.

Platform Used

Computer PIV (1.7 dual processor), 1 GB Ram, 200 GB Hard disk with software Microsoft Excel 2003.

Fabrication of Gastroretentive Acyclovir Tablets

Matrix tablets were prepared by wet granulation method. Acyclovir, polymer and Avicel were weighed and sifted together through the sieve #40 ASTM and blended in a polybag for 5 min. Blended material was granulated (what are steps/method of granulation?) using ethanolic solution of PVP-K30. The wet mass was dried in a tray dryer for 30 min at 40° C. and dried materials passed through a sieve #20 ASTM. Granules were blended with magnesium stearate and compressed using 19 mm×9 mm, modified capsules shaped, concave punch. The formulation ingredients of various batches are summarized in Table 9. The hardness of the tablets was kept in the vicinity of 19.6-22.6 kp and thickness was 5.94 and 6.03 mm.

Characterization of Tablets

The properties of the compressed acyclovir gastroretentive tablets, such as hardness, friability, thickness, weight variation, and content uniformity were determined using reported procedure. Briefly, hardness was determined by using Monsanto hardness tester. Friability was determined using Roche friability testing apparatus. Weight variation and uniformity of drug content were performed according to the IP procedures.

In Vitro Drug Release Studies of Acyclovir Gastroretentive Tablets

The in vitro dissolution studies were performed using USP-2 type dissolution apparatus at 50 rpm) and temperature was maintained at 37° C.±0.5° C. Release testing was carried out in 900 ml of different dissolution media: simulated gastric fluid (pH 1.2) and phosphate buffer (pH 6.8). An aliquot (10 mL) was withdrawn at specific time intervals and drug content was determined by UV-visible spectrophotometer) at 255 nm. It was made clear that none of the ingredients used in the tablet formulations interfered with the assay.

Water Uptake Kinetics

Water uptake studies were performed by equilibrium weight gain method using USP type I dissolution test apparatus. The tablets were accurately weighed and placed in a dissolution basket. The basket was immersed in a dissolution vessel containing 900 ml 0.1 N HCl (pH1.2) maintained at 37±0.5° C.; speed of rotation was 50 rpm. At regular intervals, the basket-matrix system was removed from the dissolution vessel, blotted with tissue paper to remove excess water, and reweighed. The percentage water uptake (i.e., the degree of swelling due to absorbed medium) was calculated using following equation.

% Water Uptake=W _(t) /W ₀×100   (2)

Where W₀ and Wt are weights of dry and swelled tablet at time t, respectively.

Matrix Erosion Studies

Matrix erosion studies were performed by a method reported by Ebube et al.²⁵ USP type I dissolution test apparatus was used for this purpose. The dry tablets were weighed, placed in dissolution basket containing 900 ml of 0.1 N HCl (pH1.2) maintained at 37±0.5° C. and the basket was rotated at 50 rpm. At regular intervals, the whole basket-matrix assembly was removed from the dissolution vessels and dried to a constant weight in a hot-air oven at 50° C. The matrix erosion (E) at time, t, was estimated from Eq. 3.

Matrix erosion %=W _(dt) _(t) /W ₀×100   (3)

Wdt and Wo are weights of dried tablet and initial weight of dry tablet at time t respectively.

Mucoadhesive Measurement Study of Acyclovir Gastroretentive Tablets

Mucoadhesive strength of acyclovir gastroretentive tablets were determined by detachment force measurement method using pig intestine. Immediately after slaughter, different parts of intestine were removed and transported to Tyrode solution kept at 4° C. The composition of tyrode Tyrode solution (g/L) is NaCl, 6; KCl, 0.2; CaCl2 2H2O, 0.134; NaHCO3, 1.0; sodium hydrogen phosphate, 0.05; glucose-H2O, 1.0. During the experiment, the solution was aerated with pure oxygen and kept at 37° C. The intestinal tissue was fixed on glass plate of receptor compartment. The tablet was placed over intestinal tissue and on the other end of the glass rod a pan was attached in which a beaker was placed. After keeping the preparation for 30 min, the water was added with a burette dropwise to the beaker. The force needed to detach the tablet was measured using a modified precision balance. The force was used as a parameter for adherence. The force F in newtons was calculated by the equation

F=0.00981W/2   (4)

Where W is the amount of water in the beaker in grams.

Statistical Analysis

Data are expressed as the mean±standard deviation (SD) of the mean. Statistical analysis was carried out employing the student's t test using the Graph-pad PRISM software (Version 2.01, San Diego, Calif.). A value of p<0.05 was considered statistically significant.

Results Preparation and in Vitro Characterization

Table 1 shows the composition of different microsphere formulations prepared using chitosan, thiolated chitosan and trimethyl chitosan as polymers and results were compared with microsphere prepared with widely used mucoadhesive polymers Carbopol 71G and Methocel K15M.

Twenty different types of microsphere formulations were prepared using four different formulations and process variables. Initially, chitosan microspheres were prepared using different drug concentrations (batch CH-A1 to CH-A5 containing 0.1 to 0.5% w/v acyclovir), different polymer concentrations (batch CH-B1 to CH-B5 containing 1.0 to 5.0% chitosan), different volume of cross linker (batch CH-C1 to CH-C5 containing 0.25 to 1.0 ml glutaraldehyde) and different speed of stirring (batch CH-D1 to CH-D5 prepared at 1200 to 2000 rpm). Optimization of each variable was carried out on the basis of their characterization in terms of surface morphology, particle size, entrapment efficiency and in-vitro drug release and data is summarized in Table 2.

Batch CH-D5 (acyclovir con. 0.3% w/w, chitosan, 2% w/v, volume of cross linker, 1.0 ml and speed of stirring at 2000 rpm) was selected as optimum batch because it exhibited high entrapment efficiency (88.0±4.1%), possessed perfectly spherical shape and sustained the drug release (71.1±2.8% drug release at 11 hr). Two batches of microsphere formulation M-TMC and M-TCH using all the above optimized values was prepared using N-Trimethyl chitosan chloride and thiolated chitosan instead of chitosan as polymer.

FIG. 1(A-E) depict the photomicrographs of microspheres prepared using chitosan, N-TMC, thiolated chitosan, Carbopol 71G and Methocel K15M polymers. All microsphere formulations were spherical in shape and possessed smooth surface as visualized under SEM. The size of different microspheres formulation was found to range from 11.2±0.4 to 21.3±1.0 μm (Table 2). The particle size was dependent mainly on the concentration of the polymer and stirring speed. Table 2 shows the effect of stirring rate on the particle size of microspheres. The results showed that increasing the stirring speed from 1200 to 2000 rpm decreased the particle size from 21.3±0.9 μm to 12.5±0.3 μm. This can be attributed to the greater energy generated at higher stirring speed, which was able to efficiently disperse the bigger droplets to smaller ones having less particle size. Increase in the concentration of polymer from 1 to 3% w/v produced a significant increase (p<0.05) in the particle size. However, thereafter further increase in polymer concentration (from 3 to 5% w/v) didn't significantly (p<0.05) influence the particle size. When the chitosan concentration was increased from 1 to 3%, the viscosity of chitosan solution increased and bigger droplets of the internal phase during emulsification step were produced. This increase is high enough to result in difficult dispersion and subdivision of droplets thus, resulting in large size of microspheres. It was observed that the volume of glutaraldehyde (cross-linker solution) did not have a significant influence (P<0.05) on the particle size and entrapment efficiency of the microspheres. On the other hand, stirring speed did significantly effect (P<0.05) the particle size of microspheres. An increase in the stirring speed from 1200 to 2000 rpm significantly decreased (p<0.05) the particle size. The geometric mean diameter decreased from 21.3±0.9 to 12.5±0.3 μm with an increase in the stirring speed. Microspheres prepared at higher stirring speed were perfectly spherical compared to lower stirring speed, which resulted in the formation of clumps. Microspheres became more discrete with increase in the stirring speed from 1200 to 2000 rpm (Table 2).

Entrapment efficiency of different microsphere formulations was found 55±1.8 to 91.6±3.1% (Table 2). Entrapment efficiency was found to be mainly dependent on the concentration of polymer used. Other formulation and process variable didn't show any significant (p<0.05) effect. The result of entrapment efficiency measurement was well correlated with the previous report of Thanoo et al.²⁶.

The production yield of optimized microsphere formulations was found to be 74.5±3.5, 72.4±2.8, 76.3±3.8, 69.4±4.1 and 54.1±3.0, respectively, for chitosan, N-TMC, thiolated chitosan, Carbopol 71G and Methocel K15M polymers. The entrapment efficiency (% w/w) of acyclovir in optimum batch of microspheres prepared from chitosan, N-TMC, thiolated chitosan, Carbopol 71G or Methocel K15M was found to be 88.0±2.6, 91.3±4.5 86.8±3.1, 91.4±4.2 and 77.3±4.2, respectively (Table 3).

Mucoadhesive Measurement

Table 3 summarized the results of mucoadhesive measurement of different microspheres formulation in pig intestine. The adhesion time of microspheres followed the rank order of thiolated chitosan (8.0±0.8 hr)>N-TMC (4.9±0.6) chitosan (3.1±0.4 hr)>Carbopol 71G (1.1±0.2)>Methocel K15M (0.2±0.1 hr). Without getting bound to any theory we have following understanding on various observations in this inventions. Comparatively poor mucoadhesion of Methocel microspheres could be attributed to its non-ionic property. On the contrary, strong electrostatic attraction seems to have contributed to good mucoadhesion between mucin and Carbopol 71G or chitosan. Numerous hydrophilic functional groups such as carboxyl groups in chitosan molecules have an ability to form hydrogen bonds with the mucus molecules. This interaction is reported to be responsible for mucoadhesive property of this polymer.²¹ N-TMC microsphere has significantly higher mucoadhesion in comparison to chitosan microsphere due to ionic nature of N-TMC bearing the positive charge that will form a strong bond with —SH group of mucin resulting in strong mucoadhesion. Carbopol microspheres possessed negative charge, which in presence of investigating medium PBS buffer (pH 6.8) could have been repelled by the negatively charged mucus leading to poor mucoadhesion.

The excellent mucoadhesion was observed in thiolated chitosan microspheres may be due to presence of thiol groups, which are known to enhance the mucoadhesive property of chitosan because of formation of strong covalent bonds (disulfide bonds) with mucin. The formation of disulfide bonds between the thiomer and the mucus gel layer takes place either through thiol/disulfide exchange reaction or via a simple oxidation process of thiol groups.²⁷ However, other polymers like chitosan or Carbopol form non-covalent bonds like hydrogen bonds, van der Waal's forces or ionic interactions thereby resulting in weak mucoadhesion.

Swelling Study

FIG. 2 shows the percentage swelling of different microsphere formulations at different time intervals. The results revealed that all microsphere formulations swelled rapidly when immersed in phosphate buffer (pH 6.8). It is reported that adhesive properties and cohesiveness of mucoadhesive polymers are generally affected by their swelling behavior.²⁸ Mucoadhesive microspheres are supposed to take up water from underlying mucosal tissue by absorbing, swelling, and capillary effects, leading to considerable stronger adhesion.²⁹ % Swelling of different microsphere formulation was found to follow the rank order 248.3±18, 260.1±20, 198.2±15, 279.1±26 and 164±15%, respectively, after 2 hr for microsphere prepared from chitosan, N-TMC, thiolated chitosan, Carbopol 71G and Methocel K15M. After 5 hr of incubation % swelling was observed to be 295.5±28, 309.2±24, 273.2±24, 340.7±30 or 173.1±15%, respectively. Chitosan and Methocel K15M microspheres showed significantly less (p<0.05) swelling as comparison to thiolated chitosan, N-TMC or Carbopol 71G microsphere. It was observed that N-TMC and thiolated chitosan microspheres swell slowly and produced higher mucoadhesive strength. This is perhaps because slow swelling avoids the formation of over hydrated structure that looses its mucoadhesive properties before reaching the target.³⁰ On the other hand, highest swelling observed in microspheres of Carbopol 71G could be due to its high ionization at pH 6.8, which is capable of absorbing high amount of water.³¹

In Vitro Drug Release

FIG. 3 shows the release of acyclovir from various mucoadhesive microspheres. Drug powder enclosed in hard gelatin capsules was completely released (95.3±4.1%) with in 1 hr. The time taken to release 75% of acyclovir (t₇₅) from chitosan, N-TMC, thiolated chitosan, Methocel K15M or Carbopol 71G micospheres was 5.0±0.4, 8.0±0.6, 9.5±0.7, 4.0±0.3 and 5.5±0.6 hr, respectively. The significantly higher time required (p<0.05) by the thiolated chitosan microspheres to release acyclovir may be due to its better stability in acidic medium, which contributed significantly less amount of drug release during initial 1 hr of dissolution (29.3±1.1% and 20.5±0.5% drug released from chitosan or thiolated chitosan microsphere during 1 hr). This initial higher release of acyclovir from chitosan microspheres may be attributed to the higher solubility of chitosan in acidic medium. Chitosan is soluble in acidic medium but crosslinking with glutaraldehyde through its amino group stabilized the microspheres matrix and provide the sustained release.²⁶ Significantly lesser drug release from thiolated chitosan microspheres is due to the presence of disulphide bonds in microsphere matrix further stabilized the structure along with glutaraldehyde as cross linking agent. Higher amount of drug released from Methocel K15M microspheres could be assigned to its linear structure and low viscosity at pH. It was surprising that whereas the microspheres of acrylamide grafted dextran and CS released 20 to 40% acyclovir in first hour itself, microspheres from trimethyl chitosan released only about 7% chitosan in the first hour leading to most uniform drug release profile over a period of 12 hours ultimately leading to 80% release in 12 hours, while microspheres from other investigated compositions released drug ranging from about 20% (for microspreres of carbopol) to about 35% (for microsperes of Methocel) in first hour.

The release rate from microsphere depend on many factors like concentration of polymer used, method of preparation, amount of cross linker used and amount of drug used, dissolution conditions etc.

For the characterization of the release kinetics the in vitro drug release data was fitted to zero order, first order and Higuchi equation

M _(t) /M _(f) =Kt ^(n)

Where, M_(t) is the amount of drug release at time t; M_(f) is the amount of drug release after infinite time; K is the release rate constant; n is the diffusional exponent indicative of the operating release mechanism.

Quantitative GIT Distribution

Table 4 shows the time course of distribution of mucoadhesive microspheres loaded with 6-CF in the GI tract, including the stomach (Section 1) and small intestine (Section 2-7) after oral administration has been determined. 6-CF was selected as fluorescence marker because of its hydrophilic nature, higher extraction efficiency (>95%) and lower detection limit (1.0 ng/ml). Following oral administration, more than 30% 6-CF solution was recovered from stomach, but less than 10% was located after 4 hr. Maximum amount of 6-CF was transferred to the lower part of intestine after 8 hrs of its administration in rats. The reason for poor retention of 6-CF at absorption site is its soluble nature and its very little affinity to GIT tissue. On the other hand oral administration of 6-CF loaded thiolated chitosan microspheres revealed a different GI distribution pattern. After 2 hr, 22.3±3.1% formulation was recovered from stomach (Section 1) and after 4 hr, nearly 41.6±2.9% was recovered from Section 2, 3 and 4 (duodenum and jejunum portion of intestine). Further, after 10 hr of administration, 26±2.1% formulation was recovered from Section 2, 3 and 4. The significantly higher quantity of acyclovir recovered (p<0.05) from sections 2, 3 and 4 of GIT suggest gastroretentive characteristic of thiolated chitosan microsphere formulation. In comparison chitosan, Carbopol 71G and Methocel K15 microspheres showed 33.5±4.2, 17±2.8 and 9.6±1.4% recovery from section 2, 3 and 4 of GIT after 4 hr of oral administration and 12.9±1.2, 2.5±0.3, 0% recovery after 10 hr of administration. The 2-fold higher GI retention of thiolated microspheres in comparison to chitosan, Carbopol 71G and Methocel K15M microsphere formulation may be attributed to the better mucoadhesive properties of thiolated chitosan in pH 5-6 that is the pH of duodenum and jejunum region of intestine.³² The main problem with the conventional therapy of acyclovir is its poor retention in duodenum and jejunum region resulting in very poor absorption of drug and nearly more than half of the drug is recovered in the faeces in unchanged form.

Qualitative GIT Distribution Study

Gastroretentive characteristic and permeation enhancement effects of microsphere formulations was determined by carrying out by determining the extent of penetration across the duodenum and jejunum section (Section 2, 3 and 4) of fluorescence marker (6-CF) loaded microspheres formulation. FIG. 4(A-F) shows the photomicrograph of rat intestine after treatment with 6-CF solution (5A), thiolated chitosan (5B), N-TMC (5C), chitosan (5D), Carbopol 71G (5E) or Methocel K15M (5F) microspheres. The fluorescence photomicrographs revealed better qualitative uptake and localization of fluorescence marker loaded mucoadhesive microsphere in duodenum and jejunum as compared to its solution. Oral administration of 6-CF loaded thiolated chitosan and N-TMC microsphere showed higher fluorescence intensity accompanied with deep penetration of marker in intestinal tissue (FIG. 5B, 5C) This indicates higher mucoadhesiveness and penetration enhancement effect of thiolated chitosan and N-TMC microsphere formulation. Thiolated chitosan and N-TMC is reported to open the tight junction of intestinal epithelium by interacting with intestinal protein this is responsible for its penetration enhancing effect.³² Acyclovir is a Class III drug. Its low permeability is the rate-limiting factor influencing its oral absorption. Hence, these results indicate that the penetration enhancement effect of thiolated chitosan microspheres could be beneficial in facilitating the oral absorption of acyclovir.

Hemolytic Toxicity Assay

Hemolytic assay is a simple method widely used to study polymer-membrane interaction. It gives a quantitative measure of hemoglobin release. Table 5 compares the results of % hemolysis of different microspheres formulations of acyclovir. Thiolated chitosan, N-TMC, chitosan, Carbopol 71 G and Methocel K15 M microspheres showed 13.1±1.2, 27.2±1.8, 20.1±2.0, 26.2±3.4 and 22.0±2.8% hemolysis, respectively after 1 hr of incubation. Thiolated chitosan microsphere displayed a lower membrane damaging effect causing a significantly lower hemoglobin release than chitosan microsphere. In the case of the thiolated chitosan microspheres the lower membrane-damaging effect in comparison to the chitosan microsphere might be explained by the formation of intra- as well as inter-molecular disulfide bonds, thus leading to a higher rigidness of the microsphere matrix. Rigid molecules have more difficulties to attach to the cellular membrane than flexible molecules and showed toxicity.³³ These findings are in good agreement with previous studies of Guggi et al.³⁴ asserting that chitosan-TBA and glucosamine-TBA conjugates have a significant less toxic effect on red blood cells in comparison to unmodified chitosan and glucosamine

Pharmacokinetic Study

FIG. 5 shows the plasma concentration profile of acyclovir after oral administration in the form of solution and microspheres. Thiolated chitosan microspheres showed superiority over the other formulations in plasma concentration at 24 hours. Nearly 4.0 times higher AUC₀₋₂₄ value of acyclovir for these microspheres (1090.7±51 ng.hour/ml) as compared to drug solution (281.7±28 ng.hour/ml) was observed. For Trimethyl chotosan microspheres, however, this value that was still higher i.e. 1335.5, rise in plasma concentration was earlier and higher, achieved highest plasma concentration at 10 and 12 hours which lowered than Thiolated chitosan at 24 hours. Thus, for a 12 hours dosing, Trimethyl Chitosan may be superior than Thiolated Chitosan, although on account of significantly low haemolytic activity, Thiolated chitosan may be considered preferable over Trimethyl chitosans and best amongst all the microsphere compositions tested here. Gastroretentive characteristic of microsphere formulations was further supported by significantly higher (p<0.05) relative bioavailability 387% for M-TCH) as compared to drug solution. In addition, thiolated chitosan microspheres showed the ability to maintain the acyclovir plasma concentration through 24 hr as compared to the drug solution that could maintain this level of drug only for 5 hr. These results confirmed the sustained release potential of mucoadhesive microspheres of acyclovir prepared from thiolated chitosan. Hence, the overall better pharmacokinetic performance of thiolated chitosan microsphere in comparison to drug solution is due to (1) increased residence time within upper GI tract as evident by GI distribution study (2) an intensified contact between the intestinal mucosa and microspheres as evident by mucoadhesion study (3) increased drug concentration at site of absorption as evident by in vitro drug release study and (4) facilitated drug permeation through mucosa as evident by fluorescence microscopy study.

Plasma Concentration Profiles of Acyclovir IR 400 mg—Single Dose

Three parameters, time for maximum plasma concentration (t_(max)), elimination half life (t_(1/2)), and area under plasma concentration profile (AUC) were collected from literature^(16, 18, 35, 36). Other pharmacokinetic parameters were calculated from these values and provided in the table 6.

A simulation was performed to calculate the plasma concentrations during the course of single dose by using the parameters described in the table 7. The C_(max) was 0.78 mcg/mL. The FIG. 6-11 shows the plasma concentration-time profile of this simulation.

Plasma Concentration Profiles of Acyclovir IR 200 mg—Single Dose

Plasma concentrations of Acyclovir IR 200 mg were calculated from the simulated blood levels of Acyclovir IR 400 mg by extrapolation. The pharmacokinetics of Acyclovir is less than dose proportional (non-linear pharmacokinetics). Hence, the plasma concentrations of 400 mg dose were not linearly extrapolated, but a ratio of 0.69 was used (200 mg:400 mg)¹. The FIG. 7 shows the comparison of simulated plasma concentration-time profiles of Acyclovir IR 200 mg & 400 mg.

Plasma Concentration Profiles of Acyclovir IR 200 mg—Multiple Dose

Plasma levels of multiple dose administration of Acyclovir IR 200 mg (200 mg every 4 hours, 5 times daily)³⁶ were simulated by super position method as shown in the FIG. 8

The FIG. 9 shows the comparison of plasma concentrations of Acyclovir IR 200 mg during the dosing day on day 1 and day 5. The difference in the maximum and minimum plasma concentrations (C_(max) and C_(min)) achieved during day 1 and day 5 was insignificant. C_(max) was about 0.80 mcg/mL and C_(min) was about 0.10 mcg/mL.

Plasma Concentration Profiles of CR Formulations

Simulation was performed by two methods. First is by considering that the release of the drug and absorption follow a zero order kinetics (ER-Zero order), and the second by considering first order (ER-First order).

Comparative plasma concentration profiles are shown in FIG. 10.

The table no 7 provides the simulated pharmacokinetic parameters of CR formulations in comparison with IR formulation. It can be observed from the data on the table above that the C_(max)/C12 h/C24 h plasma levels of CR formulations are close to that achieved after the administration of IR formulations.

An important biopharmaceutics factor that has to be noted here is the slow GI transit time during the second dose of the day where most of the course of the absorption is to take place in a lied down position and reduced gastrointestinal movements (when the patient is asleep). Usually this must result in a better bioavailability than the first dose (morning dose), but with a slow rate of absorption resulting in a lower C_(max) as compared to the morning dose.

In-Vitro Drug Release

Since the absorption of the drug after administration of CR formulation will be independent of the intrinsic absorption rate, as the intrinsic absorption rate is far higher than drug release rate from the dosage form. So, the absorption rates used for the above simulations are considered to be reflective of the drug release. Hence the in-vitro drug release from these formulations was calculated using the general equations governing zero/first order kinetics. Table 8 and FIG. 11 present the simulated in-vitro release rate.

Preparation and Characterizations of Acyclovir Gastroretentive Tablets

Table 9 shows the composition of different gastroretentive acyclovir tablets. Carbopol and PEO were selected as mucoadhesive swellable polymers for controlling the release of acyclovir. Carbopol and PEO have many advantages as candidate for extended release tablets like good gel forming ability and mucoadhesive properties. The 763 mg was selected the dose of acyclovir for controlled release tablets as calculated by simulation study (Table 8 and FIG. 11). Tablets were prepared by wet granulation method and characterized for different quality control parameters.

FIG. 12-14 shows the in vitro drug release of different batches of gastroretentive tablets. Results shows that batch Acy-ER-1A, 1B and Acy-ER-3A, 3B and 3C prolong the drug release to 12 hr period of time. FIG. 15 shows the comparative graph of in vitro drug release profile of different batches with target profile generated by computer simulation study. Batch Acy-ER-3B and Acy-ER-1B were found best match with the target release profile.

Swelling is a very important characteristic of polymer that control the drug release and increase the G.I. retention of gastroretentive tablets. FIG. 15 shows the % swelling of different batches of acyclovir tablets. Result shows that batch Acy-ER-1B and Acy-ER-3B shows the significantly higher and prolong swelling to 12 hr period of time. Acy-ER-1B and 3B shows the 302.5 and 255.7% swelling after 45 min and 34.9 and 12.2% swelling after 12 hr period of time. Results are well correlated with the in vitro drug release study where similarly drug release was prolonged for 12 hr period of time. The results also show the matrix stability to 12 hr period of time.

FIG. 16 shows the results of mucoadhesive strength measurements of different batches of gastroretentive tablets. Batch Acy-ER-1B and 3B have shown the higher mucoadhesive strengths in comparison to other batches. This invention is based on the principal of combination of swelling and mucoadhesive mechanism for preparation of gastroretentive tablets of acyclovir. Acyclovir is absorbed predominately from upper G.I tract to duodenum and jejunum region. The results of swelling and mucoadhesive measurement study showed that these both mechanisms are working in combination to develop gastroretentive tablets of this invention.

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TABLE 1 Composition of different microsphere formulation Drug Polymer Volume of Speed of Concentration Concentration Cross-Linker Stirring Form. Code (% w/w) (% w/v) (ml) (rpm) M-CH-A1 0.1 2.0 0.1 1800 M-CH-A2 0.2 2.0 0.1 1800 M-CH-A3 0.3 2.0 0.1 1800 M-CH-A4 0.4 2.0 0.1 1800 M-CH-A5 0.5 2.0 0.1 1800 M-CH-B1 0.3 1.0 0.1 1800 M-CH-B2 0.3 3.0 0.1 1800 M-CH-B3 0.3 4.0 0.1 1800 M-CH-B4 0.3 5.0 0.1 1800 M-CH-C1 0.3 2.0 0.2 1800 M-CH-C2 0.3 2.0 0.4 1800 M-CH-C3 0.3 2.0 0.6 1800 M-CH-C4 0.3 2.0 0.8 1800 M-CH-C5 0.3 2.0 1.0 1800 M-CH-D1 0.3 2.0 1.0 1200 M-CH-D2 0.3 2.0 1.0 1400 M-CH-D3 0.3 2.0 1.0 1600 M-CH-D4 0.3 2.0 1.0 2000 M-TMC 0.3 2.0 1.0 2000 M-TCH 0.3 2.0 1.0 2000 *M-CA 0.3 2.0 1.0 *M-ME 0.3 2.0 1.0 M-CH-Chitosan Microspheres; M-TMC-Trimethyl chitosan chloride microspheres; M-TCH- Thiolated chitosan microsphere, M-CA = Carbopol 71G microspheres; M-ME = Methocel K15M microsphere *Carbopol and Methocel K15M microsphere prepared using Spray drying method A1-A5-Drug concentration from 0.1 to 0.5% w/w respectively B1-B4-Polymer concentration from 1.0 to 5.0% w/w respectively C1-C5- Variation in volume of cross linker from 0.2 to 1.0 ml respectively D1-D4- Variation in speed of stirring from 1200 to 2000 rpm respectively

TABLE 2 Characterization and optimization of different microsphere formulation % Entrapment Form. Code Surface Shape Particle size efficiency M-CH-A1 − Aggregation 15.0 ± 03   55 ± 1.8 M-CH-A2 − Aggregation 17.2 ± 0.5 64.2 ± 2.8 M-CH-A3 − Aggregation 20.8 ± 0.9 74.5 ± 3.1 M-CH-A4 − Aggregation 20.0 ± 0.8 68.7 ± 2.9 M-CH-A5 − Aggregation 19.5 ± 0.6 60.9 ± 2.5 M-CH-B1 − Aggregation 12.3 ± 0.1  67 ± 2.8 M-CH-B2 + Discrete 18.1 ± 0.5 85.1 ± 3.9 M-CH-B3 + Discrete 15.0 ± 0.3 70.9 ± 2.9 M-CH-B4 + Discrete 14.9 ± 0.2 65.0 ± 2.5 M-CH-C1 + Discrete  19.5 ± 0.89 90.0 ± 4.1 M-CH-C2 + Discrete  19.0 ± 0.82 88.5 ± 3.7 M-CH-C3 + Discrete  19.2 ± 0.84 88.0 ± 3.6 M-CH-C4 + Discrete  18.9 ± 0.79 89.4 ± 3.9 M-CH-C5 + Discrete  18.8 ± 0.75 92.0 ± 4.3 M-CH-D1 ++ Discrete 21.3 ± 0.9 87.7 ± 3.7 M-CH-D2 ++ Discrete 19.1 ± 0.8 87.2 ± 3.6 M-CH-D3 ++ Discrete 17.5 ± 0.7 87.0 ± 3.5 M-CH-D4 ++ Discrete 12.5 ± 0.3 88.0 ± 2.6 M-TMC ++ Discrete 11.2 ± 0.4 91.3 ± 4.5 M-TCH ++ Discrete 21.3 ± 1.0 86.8 ± 3.1 M-CA + Aggregate 20.6 ± 1.2 91.4 ± 4.2 M-ME + Aggregate 17.8 ± 1.5 77.3 ± 4.2 Value represent as mean ± SD (n = 3) − Rough + Smooth ++ Perfectly smooth

TABLE 3 In vitro characterizations of mucoadhesive microspheres Formulation Production Particle Size Entrapment Adhesion Code Yield (%) (μm) efficiency (%) Time (Hrs) M-CH 74.5 ± 3.5 18.2 ± 0.8 88.0 ± 2.6 3.1 ± 0.4 M-TMC 72.4 ± 2.8 11.2 ± 0.4 91.3 ± 4.5 4.9 ± 0.6 M-TCH 76.3 ± 3.8 21.3 ± 1.0 86.8 ± 3.1 8.0 ± 0.8 M-CA 69.4 ± 4.1 20.6 ± 1.2 91.4 ± 4.2 0.2 ± 0.1 M-ME 54.1 ± 3.0 17.8 ± 1.5 77.3 ± 4.2 1.1 ± 0.2 Data represents as mean ± SD (n = 3)

TABLE 4a GI distribution of 6-CF in rat gastrointestinal tract after administration as solution and mucoadhesive microspheres % Dose recovered Section 6-CF solution M-TCH M-CH no. 2 hr 4 hr 6 hr 8 hr 10 hr 2 hr 4 hr 6 hr 8 hr 10 hr 2 hr 4 hr 6 hr 8 hr 10 hr 1 52.2 ±  3.5 ± 0 0 0 22.3 ± 12.6  6.8 ± 0.6  2.1 ± 0.3 0 23.8 ± 11.2 ± 0.8  4.3 ± 0.5 0 0 Stomach 2.3 0.2 3.1 1.4 2.5 2. 10.9 ± 19.5 ± 0 0 0 15.5 ± 16.3 ± 1.7 12.4 ± 1.1  7.8 ± 0.7  3.8 ± 0.2 14.2 ± 13.1 ± 1.2 10.2 ± 1.0  5.6 ±  1.2 ± Duodenum 1.4 3.2 1.6 1.3 0.5 0.2 3. 0 10.6 ± 0 0 0 13.9 ± 14.1 ± 1.3 14.2 ± 1.4 10.1 ± 1.2  9.1 ± 0.7 10.8 ± 12.6 ± 1.2 10.6 ± 1.1  8.9 ±  4.2 ± Jejunum 1.2 1.4 1.1 0.7 0.5 4. 0  5.8 ± 6.9 ± 0 0  6.4 ± 11.2 ± 1.2 15.5 ± 1.6 14.8 ± 1.6 13.1 ± 1.5  3.6 ±  7.8 ± 0.6 15.4 ± 1.4 12.1 ±  7.5 ± Jejunum 0.6 0.7 0.5 0.4 1.0 1.0 5. 0 0 3.9 ± 0 0 0  8.4 ± 0.9 15.1 ± 1.5 18.6 ± 2.0 17.5 ± 1.8 0  4.2 ± 0.5  9.6 ± 0.8 17.6 ± 13.5 ± Jejunum 0.4 1.8 1.2 6. Ileum 0 0 0 5.9 ± 0 0  4.2 ± 0.4 10.8 ± 1.1 15.5 ± 1.6 11.7 ± 1.2 0  1.5 ± 0.2  7.3 ± 0.6 15.2 ± 10.7 ± 0.7 1.4 1.0 7. 0 0 0 0 0 0  1.1 ± 0.1 10.2 ± 1.0 12.8 ± 1.2 12.1 ± 1.4 0 0  6.4 ± 0.5 13.6 ±  8.7 ± Remaining 1.2 0.7 Intestine Data represents as mean ± SD (n = 3)

TABLE 4b Continue table 4a % Dose recovered M-CA M-ME M-TMC Section no. 2 hr 4 hr 6 hr 8 hr 10 hr 2 hr 4 hr 6 hr 8 hr 10 hr 2 hr 4 hr 6 hr 8 hr 10 hr 1 Stomach 17.2 ± 5.4 ± 0.5 0 0 0 14.2 ± 1.2 0 0 0 0 22.6 ± 1.8 10.1 ± 0.8  5.2 ± 1.8 0 0 1.5 2. Duodenum  7.5 ± 7.5 ± 0.6 0 0 0  5.6 ± 0.5 2.1 ± 0.3 0 0 0 17.5 ± 1.5 12.4 ± 1.1 11.1 ± 1.0  7.1 ± 0.6  5.2 ± 0.9 0.3 3. Jejunum 0 5.8 ± 0.5 6.8 ± 0 0 0 3.5 ± 0.5 0 0 0 15.9 ± 1.2 13.6 ± 1.4 14.5 ± 1.3  8.2 ± 0.8  7.2 ± 0.7 0.6 4. Jejunum 0 3.7 ± 0.4 5.8 ± 5.4 ± 2.5 ± 0 4.0 ± 0.5 8.0 ± 0 0 10.1 ± 1.0 17.5 ± 1.5 16.3 ± 1.7 10.1 ± 1.2 10.1 ± 0.5 0.4 0.3 0.9 0.9 5. Jejunum 0 2.1 ± 0.2 4.4 ± 6.4 ± 0 0 3.2 ± 0.4 5.0 ± 0 0 0  7.5 ± 0.6 10.5 ± 0.7 11.5 ± 1.2 14.5 ± 0.3 0.5 0.5 1.1 6. Ileum 17.2 ± 5.4 ± 0.5 0 0 0 14.2 ± 1.2 0 0 0 0 0  5.1 ± 0.4 12.3 ± 1.1 13.1 ± 1.4 17.1 ± 1.5 1.5 7. Remaining  7.5 ± 7.5 ± 0.6 0 0 0  5.6 ± 0.5 2.1 ± 0.3 0 0 0 0  3.5 ± 0.2 13.5 ± 1.4 15.2 ± 1.5 20.6 ± Intestine 0.9 1.9 Data represents as mean ± SD (n = 3)

TABLE 5 Results of pharmacokinetic and hemolytic toxicity assay of different microsphere formulations of acyclovir *AUC *Cmax *MRT **RB % Form. Code (ng · hour/ml) (ng) (hr) (%) Hemolysis Drug solution 281.7 ± 28 53.07 ± 6.8  5.4 ± 0.5 100 10.2 ± 1.4 M-CH 885.8 ± 72 54.87 ± 8.2 12.4 ± 1.2 314.4 ± 13 20.1 ± 2.0 M-TMC 1335.5 ± 58  62.00 ± 8.9 13.1 ± 1.4 474.1 ± 16 27.2 ± 1.8 M-TCH 1090.7 ± 51   59.69 ± 10.1 17.9 ± 1.8 387.1 ± 18 13.1 ± 1.2 M-CA 727.8 ± 45 47.69 ± 6.8 11.6 ± 1.1 258.3 ± 12 26.2 ± 3.4 M-ME 510.5 ± 35 33.33 ± 5.8 11.3 ± 1.0 181.2 ± 10 22.0 ± 2.8 *Analyzed by WinNolin software **RB Relative Bioavailability. Data represents as mean ± SD (n = 3)

TABLE 6 Pharmacokinetic parameters of acyclovir Parameter Value Remarks Time to maximum 1.4 h From Ref. 35 plasma concentration (t_(max)) Apparent elimination 2.3 h From Ref. 35 half-life (t_(1/2)) Area under plasma 3.3075 From Ref. 35 concentration profile mcg*h/mL (AUC) Elimination rate 0.3010 h⁻¹ Calculated from t_(1/2) constant (k_(el)) Absorption rate 3.2894 h⁻¹ Calculated from t_(max). Since, (k_(a)) it is an IR product, it is assumed that almost 99% of absorption is complete at t_(max) Apparent volume 401.38 L Calculated from dose, AUC of distribution (V_(z)) and k_(el)

TABLE 7 Simulated pharmacokinetic parameters of CR formulations in comparison with IR formulation. Day 5 Day 1 CR- CR- CR-Zero CR-First Zero First Formulation IR Order Order IR Order Order Dose (mg) 1000 723 723 1000 723 723 Absorption 3.2894 h⁻¹ 100 mg/h 0.2556 h⁻¹ — — — rate C_(max) 0.80 0.80 0.88 0.80 0.80 0.89 (mcg/mL) C_(12h) 0.32 0.31 0.25 0.32 0.32 0.27 (mcg/mL) C_(24h) 0.10 0.32 0.27 0.10 0.32 0.27 (mcg/mL) AUC_(t) 11.05 13.88 13.69 — — — (mcg*h/mL) % AUC 100 126 124 — — —

TABLE 8 Predicated in vitro drug release profile of Acyclovir CR formulation % Drug Released Time (h) Zero order First order 0 0.0 0.0 1 11.1 22.6 2 22.2 40.0 3 33.3 53.6 4 44.4 64.0 5 55.6 72.1 6 66.7 78.4 7 77.8 83.3 8 88.9 87.1 9 100.0 90.0

TABLE 9 Composition of sustained release gastroretentive tablets of acyclovir Acy- Acy- Acy- Batch no. Acy-ER-1A ER-1B ER-2A Acy-ER-2B Acy-ER-3A ER-3B Acy-ER-3C Acyclovir 763.37 763.37 763.37 763.37 763.37 763.37 763.37 Carbopol 100 150 — — 50 75 25 974P *PEO — — 100 50 50 25 75 Avicel PH 93.83 43.83 93.83 143.83 93.83 93.83 93.83 101 Povidone 30 30 30 30 30 30 30 K30 Magnesium 7.5 7.5 7.5 7.5 7.5 7.5 7.5 stearate Colloidal 5.0 5.0 5.0 5.0 5.0 5.0 5.0 silicon oxide Ethanol q.s. q.s. q.s. q.s. q.s. q.s. q.s. Total 1000 mg 1000 mg 1000 mg 1000 mg 1000 mg 1000 mg weight *Polyethylene oxide 

What is claimed is:
 1. A controlled release dosage form containing no solubilizer, comprising a therapeutically effective amount of a pharmaceutically active agent, comprising: a. a tablet made from a polymer matrix of at least two biocompatible polymers, at least one of which is mucoadhesive, the pharmaceutically active agent and pharmaceutically permitted excipients; the tablet capable of rapid swelling without disintegration in a simulated gastric juice to a size that results in its gastric retention in a stomach and start a controlled release of the active agent by starting a controlled erosion immediately after coming into contact with the gastric juice, or b. microspheres of ungrafted chitosan or a chitosan derivative incorporating the active agent, wherein the pharmaceutically active agent is not a polymeric molecule and after administration in the stomach, the microspheres adhere to the gastric mucosa for a long time releasing the active agent in a controlled way, wherein: the controlled release dosage form containing no solubilizer releases in about 12 hours of between 80-100% of the active agent in a first order rate of release in a USP-2 type dissolution test.
 2. The controlled release dosage form of claim 1, wherein the controlled release dosage form is the tablet, and the USP-2 type dissolution test is done in the simulated gastric juice and the polymers are mucoadhesive, swellable polymers comprising one or more selected from the group consisting of high molecular weight non-linear polyacrylic acid polymer cross-linked with polyalkenyl polyether, polyethylene oxide, hypermellose, sodium alginate, sodium carboxymethyl cellulose, poly(meth)acrylates based co-polymers, xanthan gum.
 3. The controlled release dosage form of claim 1, wherein the controlled release dosage form is the tablet, and the active agent is Acyclovir or Acyclovir derivatives.
 4. The controlled released dosage form of claim 1, wherein said permitted pharmaceutical excipients comprise one or more selected from the group consisting of a binder, a diluent, a pH modifier, a glidant, a lubricant, a film former, an anti-adherent, a coating agent, and a colorant.
 5. A controlled release dosage form comprising a tablet made from therapeutically effective amount of Acyclovir and containing no solubilizer that releases in about 12 hours of between 80-100% of the active agent in a first order rate of release in a USP-2 type dissolution test, wherein the USP-2 type dissolution test is done in a simulated gastric juice, and the tablet comprises a polymer matrix of high molecular weight non-linear polyacrylic acid polymer cross-linked with polyalkenyl polyether, polyethylene oxide, microcrystalline cellulose and polyvinylpyrrolidone having a viscosity of 44000-54000 cps, magnesium stearate, and colloidal silicon oxide as excipient.
 6. The controlled release dosage form of claim 5 comprising, for every 1000 mg of the dosage form; i. Acyclovir in an amount of 763.37 mg, a high molecular weight polymer of acrylic acid crosslinked with allyl ethers of pentaerythritol in an amount of 100 mg, microcrystalline cellulose in amount 93.83 mg, polyvinylpyrrolidone having a viscosity of 44000-54000 cps in an amount of 30 mg, magnesium stearate in an amount of 7.5 mg, and colloidal silicon dioxide 5.0 mg, or ii. Acyclovir in an amount of 763.37 mg, a high molecular weight polymer of acrylic acid crosslinked with allyl ethers of pentaerythritol in an amount of 150 mg, microcrystalline cellulose in an amount 93.83 mg, polyvinylpyrrolidone having a viscosity of 44000-54000 cps in an amount of 30 mg, magnesium stearate in an amount of 7.5 mg, and colloidal silicon dioxide 5.0 mg, or iii. Acyclovir in an amount of 763.37 mg, a high molecular weight polymer of acrylic acid crosslinked with allyl ethers of pentaerythritol in an amount of 50 mg, polyethylene oxide in an amount of 50 mg, microcrystalline cellulose in an amount of 93.83 mg, polyvinylpyrrolidone having a viscosity of 44000-54000 cps in an amount of 30 mg, magnesium stearate in an amount of 7.5 mg, and colloidal silicon dioxide 5.0 mg.
 7. The controlled release dosage form of claim 1, wherein the controlled release dosage form is the microspheres, and the chitosan derivative is Trimethyl chitosan or Thiolated chitosan and wherein the USP-2 type dissolution test is done in HCL buffer having pH 1.2 as a dissolution medium in first hour and a phosphate buffered saline having pH 6.8 is used in next 11 hours.
 8. The controlled release dosage form of claim 1, wherein the controlled release dosage form is the microspheres, and the microspheres are packed in a sachet or are used as an ingredient to make a solid unit dosage form comprising a tablet and a capsule.
 9. A method of administering a therapeutically effective amount of a pharmaceutically active agent from a controlled release dosage form containing no solubilizer to a patient, wherein the administration is done through an oral route comprising: i. a tablet made from a polymer matrix of at least two biocompatible polymers, at least one of which is mucoadhesive, the pharmaceutically active agent and pharmaceutically permitted excipients; the tablet capable of rapid swelling without disintegration in a simulated gastric juice to a size that results in its gastric retention in a stomach and start a controlled release of the active agent by starting a controlled erosion immediately after coming into contact with the gastric juice, or ii. microspheres of ungrafted chitosan or a chitosan derivative incorporating as the active agent, wherein the pharmaceutically active agent is not a polymeric molecule and after administration in the stomach, the microspheres adhere to the gastric mucosa for a long time releasing the active agent in a controlled way, wherein: the controlled release dosage form containing no solubilizer releases in about 12 hours of between 80-100% of the active agent in a first order rate of release in a USP-2 type dissolution test.
 10. The method of claim 9, wherein the controlled release dosage form is the tablet, and the USP-2 type dissolution test is done in the simulated gastric juice and the polymers and pharmaceutically permitted excipients comprise high molecular weight non-linear polyacrylic acid polymer cross-linked with polyakenyl polyether and polyethylene oxide, microcrystalline cellulose, polyvinylpyrrolidone having a viscosity of 44000-54000, magnesium stearate, and colloidal silicon oxide.
 11. The method of claim 9, wherein the controlled release dosage form is the tablet, and the active agent is Acyclovir or Acyclovir derivatives.
 12. The method of claim 9, wherein the controlled release dosage form is the tablet, and said permitted pharmaceutical excipients comprise one or more selected from the group consisting of a binder, a diluent, a pH modifier, a glidant, a lubricant, a film former, an anti-adherent, a coating agent, and a colorant.
 13. The method of claim 9, wherein the controlled release dosage form is the tablet, and the controlled release dosage form comprises Acyclovir, high molecular weight non-linear polyacrylic acid polymer cross-linked with polyakenyl polyether, polyethylene oxide, microcrystalline cellulose, polyvinylpyrrolidone having viscosity of 44000-54000, magnesium stearate, colloidal silicon oxide.
 14. The method of claim 9, wherein for every 1000 mg of the dosage form the controlled release dosage form being the tablet comprises Acyclovir 763.37 mg, high molecular weight non-linear polyacrylic acid polymer cross-linked with polyakenyl polyether 974P 75 mg, polyethylene oxide 25 mg, microcrystalline cellulose 93.83 mg, polyvinylpyrrolidone having viscosity of 44000-54000 30 mg, magnesium stearate 7.5 mg, colloidal silicon oxide 5.0 mg.
 15. The method of claim 9, wherein the controlled release dosage form is the microspheres, and the chitosan derivative is Trimethyl chitosan or Thiolated chitosan and wherein the USP-2 type dissolution test is done in HCL buffer having pH 1.2 as a dissolution medium in first hour and a phosphate buffered saline having pH 6.8 is used in next 11 hours.
 16. The method of claim 9, wherein the controlled release dosage form is the microspheres, and the microspheres are packed in a sachet or are used as an ingredient with optional addition of other pharmaceutically permitted ingredients and excipients to make a solid unit dosage form comprising a tablet and a capsule.
 17. A process of making an oral dosage form containing no solubilizer, comprising a therapeutically effective amount of a pharmaceutically active agent, the process comprising: i. making a wet granulation of a mixture comprising the pharmaceutically active ingredient, a matrix of at least two biocompatible polymers wherein at least one of which is mucoadhesive, and excipients, adding a glidant and pressing into a tablet, or ii. preparing a solution of chitosan or a chitosan derivative in acetic acid, adding an aqueous solution of the pharmaceutically active agent, adding this mixture to continuous phase consisting of light liquid paraffin and heavy liquid paraffin (1:1) containing a surfactant under constant stirring to form a water-in-oil emulsion, adding gluteraldehyde drop wise over a period of time, continuing stirring for a period of time, separating the microspheres formed by centrifugation, washing with petroleum ether to remove liquid paraffin, suspending in a sodium bisulfite solution and stirring for a period of time to remove residual gluteraldehyde, washing finally with distilled water, drying the microspheres wherein: the controlled release dosage form containing no solubilizer releases in about 12 hours of between 80-100% of the active agent in a first order rate of release in a USP-2 type dissolution test.
 18. The process of claim 17, wherein the pharmaceutically active agent is Acyclovir, and i. under the process of (i), the polymers are high molecular weight non-linear polyacrylic acid polymer cross-linked with polyakenyl polyether, polyethylene oxide, microcrystalline cellulose, polyvinylpyrrolidone having viscosity of 44000-54000, and ii. under the process of (ii), the chitosan derivatives are selected from the group consisting of Trimethyl chitosan and Thiolated chitosan, and wherein the USP-2 type dissolution test is done in HCL buffer having pH 1.2 as dissolution medium in first hour and phosphate buffered saline having pH 6.8 is used in next 11 hours.
 19. The process of claim 18, wherein, under the process of (ii), the microspheres are packed in a sachet or are used as an ingredient with optional addition of other pharmaceutically permitted ingredients and excipients to make a solid unit dosage form comprising a tablet and a capsule. 